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Imhs

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
IMHS FDA UDI
Generic Name
Orthopaedic implantation sleeve, reusable FDA UDI
Device Name
INTRAMEDULLARY HIP SCREW CP TELESCOPING REAMER SLEEVE FDA UDI
Model / Reference
71687022 FDA UDI
Description
INTRAMEDULLARY HIP SCREW CP TELESCOPING REAMER SLEEVE FDA UDI

Identifiers

Catalog Number
71687022 FDA UDI
Primary DI / UDI-DI
03596010519061 FDA UDI
510(k) Number
K122170 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Orthopaedic implantation sleeve, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implantation sleeve, reusable

Imhs by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implantation sleeve, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b5a7fd6f-9365-4b6c-82e6-9ca4a69e8bc0 36 fields · synced Jun 8, 2026